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45848

Supelco

Dicofol solution

100 μg/mL in methanol, PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C14H9Cl5O
CAS Number:
115-32-2
Molecular Weight:
370.49
Beilstein/REAXYS Number:
1886299
EC Number:
200-659-6
MDL number:
MFCD00055271
UNSPSC Code:
41116107
PubChem Substance ID:
329756986
NACRES:
NA.24

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

single component solution

storage temp.

2-8°C

SMILES string

OC(c1ccc(Cl)cc1)(c2ccc(Cl)cc2)C(Cl)(Cl)Cl

InChI

1S/C14H9Cl5O/c15-11-5-1-9(2-6-11)13(20,14(17,18)19)10-3-7-12(16)8-4-10/h1-8,20H

InChI key

UOAMTSKGCBMZTC-UHFFFAOYSA-N

General description

Dicofol, a non-systemic organochlorine acaricide is commonly used for a variety of agricultural applications such as ornamentals, teas, vegetables, fruits and field crops.[1][2]

Application

Dicofol may be used as an analytical reference standard for the quantification of the analyte in aquatic products[1] and milk samples[2] using different chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBS5083V

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Ryo Kamata et al.
Environmental toxicology and chemistry, 29(10), 2316-2322 (2010-09-28)
To assess the possible impact of the currently used organochlorine insecticide, dicofol, on the development and reproduction of avian species, in ovo exposure experiments to its p,p' and o,p' isomers were performed using Japanese quail (Coturnix japonica) eggs. o,p'-Dicofol (0.3-100 µg/g
Shu-ying Han et al.
Chemosphere, 83(2), 131-136 (2011-02-09)
n-Octanol/water partition coefficients (P) for DDTs and dicofol were determined by reversed-phase high performance liquid chromatography (RP-HPLC) on a C(18) column using methanol-water mixture as mobile phase. A dual-point retention time correction (DP-RTC) was proposed to rectify chromatographic retention time
Ying Liu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 89, 210-215 (2012-01-21)
Because of the widespread concern that persistent organic pollutants (POPs) may be adversely affecting the health of humans, reliable assessing their toxic effects is urgently needed. We selectively study the interaction between dicofol (DCF) and trypsin by steady state and
Ying Guo et al.
Environmental pollution (Barking, Essex : 1987), 157(6), 1753-1763 (2009-01-27)
This review summarizes and analyzes available data in the literature (mostly after 2000) on the occurrence of dichlorodiphenyltrichloroethane (DDT) and its main metabolites, dichlorodiphenyldichloroethane (DDD) and chlorodiphenyldichloroethylene (DDE), in the environment of the Pearl River Delta (PRD), South China. Generally
Maher H Haeba et al.
Environmental science and pollution research international, 15(3), 222-227 (2008-05-28)
Pollution-induced endocrine disruption in vertebrates and invertebrates is a worldwide environmental problem, but relatively little is known about effects of endocrine disrupting compounds (EDCs) in planktonic crustaceans (including Daphnia magna). Aims of the present study were to investigate acute 48
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